Catalyst for the manufacture of acrylonitrile and methacrylonitrile

ABSTRACT

Olefins such as propylene and isobutylene are converted to the corresponding unsaturated nitriles, acrylonitrile, and methacrylonitrile, respectively, by reacting a mixture of the olefin, ammonia, and molecular oxygen-containing gas in the presence of a catalyst containing the oxides of bismuth, molybdenum, iron, nickel and magnesium, at least one element selected from the group comprising potassium and cesium, and optionally one element selected from the group comprising cobalt, phosphorus, manganese, tellurium, sodium, cerium, chromium, antimony and tungsten wherein the sum of cesium and potassium is at least 0.1 to 0.4.

BACKGROUND OF THE INVENTION

This is a continuation-in-part of U.S. Appl. Ser. No. 07/462,202 filedJan. 9, 1990, now U.S. Pat. No. 5,093,299.

This invention relates to an improved process and catalyst for theammoxidation of olefin-ammonia mixtures to unsaturated nitriles, andmore particularly to an improved process and catalyst for theammoxidation of propylene-ammonia and isobutylene-ammonia toacrylonitrile and methacrylonitrile, respectively. The ammoxidation isconducted in the presence of a catalyst comprising at least one elementselected from the group comprising potassium and cesium, and the oxidesof bismuth, molybdenum, iron, nickel, and magnesium, and optionally incombination with at least one element selected from the group of cobalt,phosphorus, manganese, tellurium, sodium, cerium, chromium, antimony andtungsten.

There are many patents related to the production of acrylonitrile by useof bismuth-molybdenum-iron fluidized bed catalyst (e.g., 3,642,930). Inparticular, U.S. Pat. No. 4,863,891, issued Sep. 5, 1989, and U.S. Pat.No. 4,767,878, issued Aug. 30, 1988, disclose a process foracrylonitrile production using a catalyst comprised of the oxidesbismuth, molybdenum, iron, magnesium and optionally the oxides ofcobalt, nickel, phosphorous, arsenic and an alkali metal present in anamount less than 0.1.

The catalyst employed in the process of this invention has high activityfor the production of unsaturated nitriles at a slightly lower reactiontemperature than is normally employed for this type of process, andcontinues efficient low temperature operation after aging. In additionto high activity for nitrile production, the catalyst has a number ofother important advantages that contribute greatly to the efficient andeconomic operation of the process. The catalyst has excellent redoxstability under the reaction conditions of the process. This permits theuse of low process air to olefin ratios and high weight hourly spacevelocities. The catalyst exhibits efficient ammonia utilization thusgreatly reducing the amount of unreacted ammonia appearing in thereactor effluent and thus lowering the amount of sulfuric acid requiredto neutralize the ammonia in the effluent. This results in improvementsin (1) the operation of the recovery section of the process and (2)pollution control. The use of lower operating temperatures favors longercatalyst life and minimizes effluent problems such as afterburning.Despite the lower reaction temperatures, per pass conversions to thenitrile product of 84 percent and above are obtained. A furtherimportant advantage associated with the catalyst of this invention isthe low cost of the essential catalytic components and the ease ofcatalyst preparation.

The reactants employed in producing the unsaturated nitriles of thisinvention are oxygen, ammonia, and an olefin having three carbon atomsin a straight chain such as propylene or isobutylene, and mixturesthereof.

The olefins may be in a mixture with paraffinic hydrocarbons, such asethane, propane, butane and pentane; for example, a propylene-propanemixture may constitute the feed. This makes it possible to use ordinaryrefinery streams without special separation. Likewise, diluents such asnitrogen and oxides of carbon may be present in the reaction mixturewithout deleterious effect.

In its preferred aspect, the process comprises contacting a mixturecomprising propylene or isobutylene, ammonia and oxygen with thecatalyst at an elevated temperature and at atmospheric or nearatmospheric pressure to produce acrylonitrile or methacrylonitrile. Mostpreferably, the process is directed to contacting propylene, ammonia andoxygen with a fluid bed catalyst at an elevated temperature to produceacrylonitrile.

Any sources of oxygen may be employed in this process. For economicreasons, however, it is preferred that air be employed as the source ofoxygen. From a purely technical viewpoint, relatively pure molecularoxygen will give equivalent results. The molar ratio of oxygen to theolefin in the feed to the reaction vessel should be in the range of0.5:1 to 4:1 and a ratio of about 1:1 to 3:1 is preferred.

The molar ratio of ammonia to olefin in the feed to the reaction mayvary between about 0.5:1 to 5:1. There is no real upper limit for theammonia-olefin ratio, but there is generally no reason to exceed a ratioof 5:1. At ammonia-olefin ratios appreciably less than thestoichiometric ratio of 1:1, various amounts of oxygenated derivates ofthe olefin will be formed. Outside the upper limit of this range onlyinsignificant amounts of aldehydes and acids will be produced, and onlyvery small amounts of nitriles will be produced at ammonia-olefin ratiosbelow the lower limit of this range. It is surprising that within theammonia-olefin range stated, maximum utilization of ammonia is obtained,and this is highly desirable. It is generally possible to recycle anyunreacted olefin and unconverted ammonia.

We have found that in some cases water in the mixture fed to thereaction vessel improves the selectivity of the reaction and yield ofnitrile. However, addition of water to the feed is not essential in thisinvention, inasmuch as water is formed in the course of the reaction.

In general, the molar ratio of added water to olefin, when water isadded, is above about 0.25:1. Ratios on the order of 1:1 to 4:1 areparticularly desirable, but higher ratios may be employed, i.e., up toabout 10:1.

The reaction is carried out at a temperature within the range of fromabout 260° to about 600° C. The preferred temperature range is fromabout 310° to 500° C., especially preferred being from about 315° to480° C.

The pressure at which the reaction is conducted is another variable, andthe reaction is preferably carried out at about atmospheric or aboveatmospheric (2 to 5 atmospheres) pressure.

The apparent contact time is not critical, and contact times in therange of from 0.1 to about 50 seconds may be employed. The optimumcontact time will, of course, vary depending upon the olefin beingreacted, but in general, a contact time of from 1 to 15 seconds ispreferred.

Generally any apparatus of the type suitable for carrying outoxidation/ammoxidation reactions in the vapor phase may be employed inthe execution of this process. The process may be conducted eithercontinuously or intermittently. The catalyst bed may be a fixed-bedemploying a large particulate or pelleted catalyst or preferably, aso-called "fluidized" bed of catalyst may be employed. Any conventionalfluid ammoxidation reactor may be utilized in the practice of theprocess of the present invention. For example, the reactor described inU.S. Pat. No. 3,230,246, issued Jan. 18, 1966 incorporated herein byreference would be suitable in the practice of the present invention.

The reactor may be brought to the reaction temperature before or afterthe introduction of the reaction feed mixture. However, in a large scaleoperation it is preferred to carry out the process in a continuousmanner, and in such a system the circulation of the unreacted olefin iscontemplated. Periodic regeneration or reactivation of the catalyst isalso contemplated, and this may be accomplished, for example, bycontacting the catalyst with air at an elevated temperature.

The products of the reaction may be recovered by any of the methodsknown to those skilled in the art. One such method involves scrubbingthe effluent gases from the reactor with cold water or an appropriatesolvent to remove the products of the reaction. If desired, acidifiedwater can be used to absorb the products of reaction and neutralizeunconverted ammonia. The ultimate recovery of the products may beaccomplished by conventional means. The efficiency of the scrubbingoperation may be improved when water is employed as the scrubbing agentby adding a suitable wetting agent in the water. Where molecular oxygenis employed as the oxidizing agent in this process, the resultingproduct mixture after the removal of the nitriles may be treated toremove carbon dioxide, with the remainder of the mixture containing theunreacted olefin and oxygen being recycled through the reactor. In thecase where air is employed as the oxidizing agent in lieu of molecularoxygen, the residual product after separation of the nitriles and othercarbonyl products may be scrubbed with a non-polar solvent, e.g., ahydrocarbon fraction in order to recover unreacted olefin, and in thiscase the remaining gases may be discarded. The addition of a suitableinhibitor to prevent polymerization of the unsaturated products duringthe recovery steps is also contemplated.

The catalyst useful in the process of the present invention is amixture, compound or possibly complex of the oxides of iron, bismuth,molybdenum, nickel and magnesium, at least one or more element selectedfrom potassium and cesium, and optionally one or more elements selectedfrom the group comprising cobalt, manganese, chromium, phosphorous,antimony, tellurium, sodium, cerium and/or tungsten. The composition ischaracterized by in the following empirical formula:

    A.sub.a K.sub.b Cs.sub.c Mg.sub.d Ni.sub.e Fe.sub.f Bi.sub.g Mo.sub.12 O.sub.x

wherein A is one or more of the elements selected from the groupcomprising cobalt, manganese, chromium, phosphorus, antimony, tellurium,sodium, cerium and tungsten wherein (a) is a number from 0 to 5, (b) isa number from greater than 0 to 0.4, (c) is a number from greater than 0to 0.4, provided that the sum of (b) and (c) is from 0.1 to 0.4, (d),(e), (f), and (g) are a number from about 0.2 to 10, and (x) is a numberdetermined by the valence requirements of the other elements present.Preferably, (b) is from greater than 0 to less than 0.4 and (c) is fromgreater than 0 to less than 0.4. Especially preferred are (b) from about0.05 to 0.4 and (c) from about 0.05 to 0.4. Preferably, the sum of (b)and (c) is a number from greater than 0.1 to 0.4. More preferably thesum of (b) and (c) is a number from 0.11-0.3.

The catalyst of this invention may be prepared by any of the numerousmethods of catalyst preparation which are known to those skilled in theart. For example, the catalyst may be manufactured by co-precipitatingthe various ingredients. The co-precipitated mass may then be dried andground to an appropriate size. Alternately, the co-precipitated materialmay be slurried and spray-dried in accordance with conventionaltechniques. The catalyst may be extruded as pellets or formed intospheres in oil as is well-known in the art. Alternatively, the catalystcomponents may be mixed with the support in the form of the slurryfollowed by drying, or they may be impregnated on silica or othersupports.

A particularly attrition-resistant form of the catalyst may be preparedby adding the support material to the catalyst in two stages, first bypreparing and heat-treating a mixture of active catalyst components andfrom 0 to 60% by weight of the total support material, followed byadding the remainder of the support material to the powdered form of theheat-treated catalyst.

Potassium, cesium, and sodium may be introduced into the catalyst as anoxide or as any salt which upon calcination will yield the oxide.Preferred salts are the nitrates which are readily available and easilysoluble.

Bismuth may be introduced into the catalyst as an oxide or as any saltwhich upon calcination will yield the oxide. Preferred are thewater-soluble salts which are easily dispersible within the catalyst andwhich form stable oxides upon heat-treating. An especially preferredsource for introducing bismuth is bismuth nitrate which has beendissolved in a dilute solution of HNO₃.

To introduce the iron component into the catalyst one may use anycompound of iron which, upon calcination, will result in the oxides. Aswith the other elements, water-soluble salts are preferred for the easewith which they may be uniformly dispersed within the catalyst. Mostpreferred is ferric nitrate. Cobalt, nickel and magnesium may besimilarly introduced. However, magnesium may also be introduced into thecatalyst as an insoluble carbonate or hydroxide which upon heat-treatingresults in an oxide.

To introduce the molybdenum component, any molybdenum oxide such as thedioxide, trioxide, pentoxide, or sesquioxide may be used; more preferredis a hydrolyzable or decomposable molybdenum salt. The most preferredstarting material is ammonium heptamolybdate.

Phosphorus may be introduced as an alkali metal salt, an alkaline earthmetal salt or the ammonium salt, but is preferably introduced asphosphoric acid.

Other elements may be introduced, starting with the metal, oxidizing themetal with an oxidizing acid such as nitric acid, and then incorporatingthe nitrate into the catalyst. Generally, however, the nitrates arereadily available and form a very convenient starting material.

Other variations in starting materials will suggest themselves to oneskilled in the art, particularly when the preferred starting materialsmentioned hereinabove are unsuited to the economics of large-scalemanufacture. In general, any compounds containing the desired catalystcomponents may be used provided that they result in the oxides of theinstant catalyst upon heating to a temperature within the rangedisclosed hereinafter.

The catalyst can be employed without a support and will displayexcellent activity. The catalyst can also be combined with a support,and preferably it is combined with at least 10 percent up to about 90percent of the supporting compound by weight of the entire composition.Any known support materials can be used, such as, silica, alumina,zirconia, titania, alundum, silicon carbide, alumina-silica, theinorganic phosphates such as aluminum phosphate, silicates, aluminates,borates, carbonates, and materials such as pumice, montmorillonite, andthe like that are stable under the reaction conditions to be encounteredin the use of the catalyst. The preferred support is silica, which isadded to the slurry during the preparation of the catalyst in the formof silica sol or fumed silica. The level of support is usually in therange of 10-70% weight present. Preferably, the level of support is inthe range of 40-60% weight present.

The catalytic activity of the system is enhanced by heating at anelevated temperature. Generally, the catalyst mixture is spray dried ata temperature of between about 110° C. to 350° C. and then heat treatedin stages for from about one to twenty-four hours or more at atemperature of from about 260° to about 1000° C., preferably from300°-400° C. to 550°-700° C.

In general, activation of the catalyst is achieved in less time athigher temperatures. The sufficiency of activation at any given set ofconditions is ascertained by a spot test of a sample of the material forcatalytic activity. Activation is best carried out in an open chamber,permitting circulation of air or oxygen, so that any oxygen consumed canbe replaced.

Further, pre-treatment or activation of the catalyst before use with areducing agent such as ammonia in the presence of a limited amount ofair at a temperature in the range of 260° to 540° C. is also beneficial.

A preferred method of preparing the catalyst of this invention and amore complete description of the process of the invention can beobtained from the following examples. In addition to the production ofunsaturated nitriles, the catalyst of this invention is also useful forthe conversion of olefins, such as propylene and isobutylene, to thecorresponding unsaturated aldehydes and unsaturated carboxylic acids.

EXAMPLES 1 TO 13

The catalysts employed in the examples of this invention were preparedby essentially the same procedure as described herein below, using theappropriate starting materials.

Fe(NO₃)₃ *9H₂ O was dissolved in H₂ O on a hot plate. The other nitrateswere then added in the following order; Mn(NO₃)₂ -50%Sol., Bi(NO₃)₃ *5H₂O, Ni(NO₃)₂ *6H₂ O, Mg(NO₃)₂ *6H₂ O, KNO₃ -10% Soln., and CsNO₃ -10%Soln. A dark greenish brown solution was formed which was maintained atapproximately 60° C. (NH₄)₆ Mo₇ O₂₄ *4H₂ O was dissolved in H₂ O, atapproximately 60° C. A silica sol (a highly dispersed colloidal silica)was added, followed by addition of CrO₃ (which had been dissolved in H₂O). Next, the nitrate solution was added to form a greenish yellowslurry, which was then evaporated on a hot plate with constant stirringuntil thickening occurred. The next step involved drying at about 120°C. Following drying, the catalyst was denitrified by heating at 290° C.for 3 hours, followed by heating at 425° C. for 3 hours, and finallycalcining at about 610° C. for 3 hours. Table I shows the startingmaterials for each example catalyst prepared by the above describedprocedure.

                                      TABLE I                                     __________________________________________________________________________    STARTING MATERIALS FOR CATALYST FORMATION (Grams)                             __________________________________________________________________________    Exam-          Ni(NO.sub.3).sub.2 *                                                                     Mg(NO.sub.3).sub.2 *                                                                Co(NO.sub.3).sub.2 *                                                                Fe(NO.sub.3).sub.3 *                    ple  KNO.sub.3                                                                          CsNO.sub.3                                                                         6H.sub.2 O                                                                          NaNO.sub.3                                                                         6H.sub.2 O                                                                          6H.sub.2 O                                                                          9H.sub.2 O                              __________________________________________________________________________    1    *0.61                                                                              *0.88                                                                              21.81 --   7.69  --    10.91                                   2    *1.36                                                                              *2.05                                                                              21.81 --   7.69  --    10.91                                   3     0.61                                                                               0.88                                                                              21.81 --   7.69  --    10.91                                   4    *0.30                                                                              *0.29                                                                              17.45 --   9.62  2.18  12.12                                   5    *2.27                                                                              *1.46                                                                              17.45 --   9.62  2.18  12.12                                   6     0.76                                                                               1.46                                                                              17.45 --   9.62  2.18  12.12                                   7    *0.45                                                                              --   21.81 0.64 7.69  --    15.15                                   8    *3.79                                                                              --   21.81 0.64 7.69  --    15.15                                   9    *3.03                                                                              *0.44                                                                              21.81 0.64 7.69  --    15.15                                   10    1.14                                                                              *2.92                                                                              21.81 0.64 7.69  --    15.15                                   11    1.36                                                                              --   23.99 --   9.62  --    12.12                                   12    0.91                                                                               1.46                                                                              23.99 --   9.62  --    12.12                                   13    0.76                                                                               1.75                                                                              23.99 --   9.62  --    12.12                                   __________________________________________________________________________    Exam-                                                                             Mn(NO.sub.3).sub.2 --                                                                Bi(NO.sub.3).sub.3 *                                                                H.sub. PO.sub.4 --                                                                 WO.sub.3 --                                                                        CrO.sub.    SiO.sub.2 Sol                          ple 50% Soln                                                                             5H.sub.2 O                                                                          85% Soln                                                                           85% Soln                                                                           CrO.sub.3                                                                         (NH.sub.4).sub.6 Mo.sub.7 O.sub.24                                                    -40%                                   __________________________________________________________________________    1   2.42   3.27  --   --   0.68                                                                              31.78   93.29                                  2   2.42   3.27  --   --   0.68                                                                              31.78   93.59                                  3   2.42   3.27  --   --   0.68                                                                              31.78   95.36                                  4   --     3.64  --   2.05 --  31.78   95.36                                  5   --     3.64  --   2.05 --  31.78   95.80                                  6   --     3.64  --   2.05 --  31.78   98.79                                  7   --     5.46  0.86 --   --  31.78   97.06                                  8   --     5.46  0.86 --   --  31.78   97.45                                  9   --     5.46  0.86 --   --  31.78   97.44                                  10  --     5.46  0.86 --   --  31.78   98.86                                  11  --     7.28  0.17 --   --  31.78   98.51                                  12  --     7.28  0.17 --   --  31.78   98.72                                  13  --     7.28  0.17 --   --  31.78   98.76                                  __________________________________________________________________________     * = 10% Solution.                                                        

In the examples given, percent conversion to the unsaturated nitrile isdefined as follows:

Mole percent per pass conversion (PPC) to unsaturated nitrile= ##EQU1##

Ammoxidation reactions carried out with the catalyst compositions ofthis invention employing propylene as the hydrocarbon feeds aresummarized in Table II. Each reaction was run in a 3/8 inch diameterstainless steel microreactor. A 3.7 gram sample of 20-35 mesh catalystwas employed. The data in these tables show that per pass conversions toacrylonitrile obtained with catalysts of the present invention aresubstantially higher than those obtained with catalysts of the priorart.

                                      TABLE II                                    __________________________________________________________________________    CONVERSION OF PROPYLENE TO ACRYLONITRILE                                                     Fixed - Bed Reactor                                                           Reaction Temperature: 430° C.                                          Contact Time: 6.0 seconds                                                     Run Time: 30 minutes                                                          Feed Ratio (Molar) C.sub.3.sup.═/NH.sub.3 /O.sub.2                        /N.sub.2 /H.sub.2 O = 1.8/2.2/3.6/2.4/6                        Exam-                                        Acrylonitrile                    ple Catalyst Composition             C.sub.3.sup.═ Conversion                                                          % Yield                                                                            % Selectivity               __________________________________________________________________________    *1. 50% K.sub.0.04 Cs.sub.0.03 Ni.sub.5 Mg.sub.2 Fe.sub.1.8 Mn.sub.0.45           Bi.sub.0.45 Cr.sub.0.45 Mo.sub.12 O.sub.x + 50% SiO.sub.2                                                      100.0   78.6 78.6                         2. 50% K.sub.0.09 Cs.sub.0.07 Ni.sub.5 Mg.sub.2 Fe.sub.1.8 Mn.sub.0.45           Bi.sub.0.45 Cr.sub.0.45 Mo.sub.12 O.sub.x + 50% SiO.sub.2                                                      98.8    84.2 85.2                        *3. 50% K.sub.0.4 Cs.sub.0.3 Ni.sub.5 Mg.sub.2 Fe.sub.1.8 Mn.sub.0.45             Bi.sub.0.45 Cr.sub.0.45 Mo.sub.12 O.sub.x + 50% SiO.sub.2                                                      19.4    15.2 78.5                        *4. 50% K.sub.0.02 Cs.sub.0.01 Ni.sub.4 Co.sub.0.5 Mg.sub.2.5 Fe.sub.2            Bi.sub.0.5 W.sub.0.5 Mo.sub.12 O.sub.x + 50% SiO.sub.2                                                         99.1    73.9 74.5                         5. 50% K.sub.0.15 Cs.sub.0.05 Ni.sub.4 Co.sub.0.5 Mg.sub.2.5 Fe.sub.2            Bi.sub.0.5 W.sub.0.5 Mo.sub.12 O.sub.x + 50% SiO.sub.2                                                         94.0    80.3 85.4                        *6. 50% K.sub.0.50 Cs.sub.0.50 Ni.sub.4 Co.sub.0.5 Mg.sub.2.5 Fe.sub.2            Bi.sub.0.5 W.sub.0.5 Mo.sub.12 O.sub.x + 50% SiO.sub.2                                                         22.7    17.0 75.0                        *7. 50% K.sub.0.03 Na.sub.0.5 Ni.sub.5 Mg.sub.2 Fe.sub.2.5 Bi.sub.0.75            P.sub.0.5 Mo.sub.12 O.sub.x + 50% SiO.sub.2                                                                    95.3    69.5 72.6                         8. 50% K.sub.0.25 Na.sub.0.5 Ni.sub.5 Mg.sub.2 Fe.sub.2.5 Bi.sub.0.75            P.sub.0.5 Mo.sub.12 O.sub.x + 50% SiO.sub.2                                                                    95.3    72.8 76.4                         9. 50% K.sub.0.20 Cs.sub.0.015 Na.sub.0.5 Ni.sub.5 Mg.sub.2 Fe.sub.2.5           Bi.sub.0.75 P.sub.0.5 Mo.sub.12 O.sub.x + 50% SiO.sub.2                                                        94.9    72.8 76.7                        *10.                                                                              50% K.sub.0.75 Cs.sub.0.1 Na.sub.0.5 Ni.sub.5 Mg.sub.2 Fe.sub.2.5             Bi.sub.0.75 P.sub.0.5 Mo.sub.12 O.sub.x + 50% SiO.sub.2                                                        47.3    35.2 74.4                        *11.                                                                              50% K.sub.0.09 Ni.sub.5.5 Mg.sub.2.5 Fe.sub.2.0 Bi.sub.1.0 P.sub.0.1          Mo.sub.12 O.sub.x + 50 wt. % SiO.sub.2                                                                         99.6    76.0 76.3                        12. 50% Cs.sub.0.05 K.sub.0.06 Ni.sub.5.5 Mg.sub.2.5 Fe.sub.2.0 Bi.sub.1.0         P.sub.0.1 Mo.sub.12.0 O.sub.x + 50 wt. % SiO.sub.2                                                            99.0    78.5 79.3                        13. 50% Cs.sub.0.06 K.sub.0.05 Ni.sub.5.5 Mg.sub.2.5 Fe.sub.2.0 Bi.sub.1.0         P.sub.0.1 Mo.sub.12.0 O.sub.x + 50 wt. % SiO.sub.2                                                            99.1    77.4 78.1                        __________________________________________________________________________     *Comparative examples                                                    

What is claimed:
 1. A catalyst composition comprising a complex of thecatalytic oxides of iron, bismuth, molybdenum, nickel, magnesium,cesium, potassium, and optionally one or more of cobalt, manganese,chromium, phosphorous, antimony, tellurium, sodium, cerium and/ortungsten and having the formula:

    A.sub.a K.sub.b Cs.sub.c Mg.sub.d Ni.sub.e Fe.sub.f Bi.sub.g Mo.sub.12 Ox

wherein A is one or more of Co, Mn, Cr, P, Sb, Te, Na, Ce, or Wwherein ais a number from 0 to 5.0; b is a number from greater than 0 to 0.4; cis a number from greater than 0 to 0.4; provided that the sum of b and cis from 0.1 to 0.4; d, e, f and g are numbers from 0.2 to 10; and x is anumber determined by the valence requirements of the other elementspresent.
 2. The catalyst composition of claim 1, wherein said catalystconsists essentially of:

    A.sub.a K.sub.b Cs.sub.c Mg.sub.d Ni.sub.e Fe.sub.f Bi.sub.g Mo.sub.12 Ox


3. The composition of claim 1 wherein said catalyst consists of:

    A.sub.a K.sub.b Cs.sub.c Mg.sub.d Ni.sub.e Fe.sub.f Bi.sub.g Mo.sub.12 Ox


4. The composition of claim 1 wherein said catalyst is supported on acatalyst support material selected from the group consisting of silica,alumina or mixtures thereof.